Medical Safety Associate - Nuernberg, Deutschland - Novocure

Novocure

Geprüftes Unternehmen

Nuernberg, Deutschland

vor 1 Woche

Geschrieben von:

Lena Wagner

beBee Recruiter

Beschreibung

Location:

Munchen, DE, Description:

Novocure is a global publiclytraded commercialstage oncology company developing a profoundly different cancer treatment therapy called tumor treating fields (TTFields) for patients with solid tumors. TTFields therapy is a noninvasive, novel, antimitotic treatment modality which utilizes proprietary technology attempting to slow or reverse tumor progression by inducing tumor cell death. Novocure's commercialized product, Optune, is approved for the treatment of adult patients with glioblastoma (GBM) in the USA, Europe and Israel. Novocure has ongoing or completed clinical trials and is further expanding its efforts into several other solid tumor indications nonsmall cell lung cancer, pancreatic cancer, ovarian cancer and other types of solid cancers.

To support our team in Munich, Germany we are looking for a

Medical Safety Associate

The
Medical Safety Associate is a position assisting in managing the mandatory safety reporting requirements for the commercial program and other functions of the Medical Safety Group (MSG) within the Global Commercialization Team.

Your responsibilities:

Investigate medical complaints received within the commercial program
Manage medical data input into the safety database
Perform review of Medical Records for complaint information
Support Literature review activities
Execute the processing and defined work flow steps of medical complaint information received by the MSG and the preparation of internal and external reports
Evaluate medical complaint information from worldwide sources and ensure followup information is requested within predetermined timelines
Communicate with healthcare professionals to collect, evaluate, and document information on reported medical complaints as needed using medical knowledge, experience and communication skills
Write medical case narratives
Support the review of medical complaints received by MSG for completeness and consistency
Participate in the compilation of aggregate reports per USA and international regulations
Compliance with corporate and department SOPs and conventions while maintaining a working knowledge of global medical device safety guidelines and requirements
Participate in special projects as assigned

Your profile:

Minimum qualifications: Bachelor's level degree preferably in Life Sciences, nursing, pharmacy or other health related profession;
1 year experience in pharmaceutical/medical device company and/or minimum 12 years in a healthcare setting
Ability to understand and evaluate technical, scientific and medical information
Demonstrate competence in obtaining, analyzing, disseminating and reporting safety information in compliance with applicable regulations
Ability to analyze case and query data and communicate results and propose recommendations
Ability to effectively communicate with healthcare professionals
Highly organized and demonstrates understanding of workflow prioritization
Ability to multitask and triage as needed
Work with others in contributing to the overall success of the company
Fluency in German and English, Written and Spoken.